6lyh
From Proteopedia
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<StructureSection load='6lyh' size='340' side='right'caption='[[6lyh]], [[Resolution|resolution]] 3.15Å' scene=''> | <StructureSection load='6lyh' size='340' side='right'caption='[[6lyh]], [[Resolution|resolution]] 3.15Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[6lyh]] is a 8 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6LYH OCA]. For a <b>guided tour on the structure components</b> use [ | + | <table><tr><td colspan='2'>[[6lyh]] is a 8 chain structure with sequence from [https://en.wikipedia.org/wiki/Camellia_sinensis_var._assamica Camellia sinensis var. assamica]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6LYH OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6LYH FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=EXU:1,3,7-trimethyl-9H-purine-2,6,8-trione'>EXU</scene>, <scene name='pdbligand=SAH:S-ADENOSYL-L-HOMOCYSTEINE'>SAH</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.1500032Å</td></tr> |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EXU:1,3,7-trimethyl-9H-purine-2,6,8-trione'>EXU</scene>, <scene name='pdbligand=SAH:S-ADENOSYL-L-HOMOCYSTEINE'>SAH</scene></td></tr> |
| + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6lyh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6lyh OCA], [https://pdbe.org/6lyh PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6lyh RCSB], [https://www.ebi.ac.uk/pdbsum/6lyh PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6lyh ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/TCS1_CAMSI TCS1_CAMSI] Involved in the biosynthesis of caffeine (PubMed:10984041, PubMed:16333668, PubMed:26773541, PubMed:30303011, PubMed:25133732). Catalyzes the conversion of 7-methylxanthine (7mX) to theobromine and of theobromine to caffeine (PubMed:10984041, PubMed:16333668, PubMed:26773541, PubMed:30303011, PubMed:25133732). Has 3-N- and 1-N-methylation activity (PubMed:10984041, PubMed:16333668).<ref>PMID:10984041</ref> <ref>PMID:16333668</ref> <ref>PMID:25133732</ref> <ref>PMID:26773541</ref> <ref>PMID:30303011</ref> | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | Caffeine is a major component of xanthine alkaloids and commonly consumed in many popular beverages. Due to its occasional side effects, reduction of caffeine in a natural way is of great importance and economic significance. Recent studies reveal that caffeine can be converted into non-stimulatory theacrine in the rare tea plant Camellia assamica var. kucha (Kucha), which involves oxidation at the C8 and methylation at the N9 positions of caffeine. However, the underlying molecular mechanism remains unclear. Here, we identify the theacrine synthase CkTcS from Kucha, which possesses novel N9-methyltransferase activity using 1,3,7-trimethyluric acid but not caffeine as a substrate, confirming that C8 oxidation takes place prior to N9-methylation. The crystal structure of the CkTcS complex reveals the key residues that are required for the N9-methylation, providing insights into how caffeine N-methyltransferases in tea plants have evolved to catalyze regioselective N-methylation through fine tuning of their active sites. These results may guide the future development of decaffeinated drinks. | ||
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| + | Identification and characterization of N9-methyltransferase involved in converting caffeine into non-stimulatory theacrine in tea.,Zhang YH, Li YF, Wang Y, Tan L, Cao ZQ, Xie C, Xie G, Gong HB, Sun WY, Ouyang SH, Duan WJ, Lu X, Ding K, Kurihara H, Hu D, Zhang ZM, Abe I, He RR Nat Commun. 2020 Mar 19;11(1):1473. doi: 10.1038/s41467-020-15324-7. PMID:32193380<ref>PMID:32193380</ref> | ||
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| + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
| + | </div> | ||
| + | <div class="pdbe-citations 6lyh" style="background-color:#fffaf0;"></div> | ||
| + | == References == | ||
| + | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| + | [[Category: Camellia sinensis var. assamica]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
| - | [[Category: Wang | + | [[Category: Wang Y]] |
| - | [[Category: Zhang | + | [[Category: Zhang Z-M]] |
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Current revision
Crystal structure of tea N9-methyltransferase CkTcS in complex with SAH and 1,3,7-trimethyluric acid
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